Hydroxychloroquine Sulfate
- Product NDC
- 71610-507
- 11-digit product format
- 716100507
- Labeler code
- 71610
- Product ID
- 71610-507_eaefffa9-a606-427c-bda6-441db98954b9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxychloroquine Sulfate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA040274
- Marketing category
- ANDA
- Marketing start
- 1998-06-18
- Marketing end
- 0000-00-00
- Substance
- HYDROXYCHLOROQUINE SULFATE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Antirheumatic Agent [EPC],Antimalarial [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71610-507-30 | 71610050730 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-507-30) | 2020-12-21 | 0000-00-00 | No | No | Current |
| 71610-507-53 | 71610050753 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-507-53) | 2020-12-21 | 0000-00-00 | No | No | Current |